Evaluation of Artesunate and Praziquantel Combination Therapy in Murine Schistosomiasis mansoni

被引:1
作者
Hegazy, Laila Abdel Moniem [1 ]
Al Motiam, Mona Hussein [1 ]
Abd El-Aal, Naglaa Fathy [1 ]
Ibrahim, Shereen Mahmoud [1 ]
Mohamed, Heba Khalil [2 ]
机构
[1] Zagazig Univ, Fac Med, Dept Med Parasitol, Zagazig, Egypt
[2] TBRI, Dept Pathol, Giza, Egypt
关键词
Schistosoma mansoni; Artesunate; Praziquantel; Apoptosis; P53; Bcl-2; CELL-DEATH; MICE; ARTEMETHER; INFECTION; LIVER; SUSCEPTIBILITY; APOPTOSIS; EFFICACY; PROTEIN; ISOLATE;
D O I
暂无
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Background: Despite the global efforts to control schistosomiasis, still prevalence in endemic regions unchanged. The present study was conducted to investigate the possible role of artesunate (AS) and praziquantel (PZQ) combination in enhancing cure in pre-patent and patent Schistosoma mansoni infection, and study the role of apoptosis in evaluation of the drugs efficacy. Methods: Eighty laboratory-bred Swiss albino male mice were classified into four groups (20 mice each); control, PZQ treated (500 mg/kg), AS treated (400 mg/kg) and combined AS (400 mg/kg) + PZQ (500 mg/g) groups. Efficacy of the drugs was assessed by parasitological (egg count/gram stool, worm burden, tissue egg load, oogram pattern), histopathological (haematoxylin and eosin - for detection of type of hepatic granulomas, number & diameter) and immunohistochemical studies (P53 and Bcl-2 markers for determination of inflammatory cells and the degree of apoptosis). Results: Significant reduction was recorded in stool egg count, tissue egg count (liver and intestine), worm burden, granuloma number and size and changed oogram patterns in artesunate - praziquantel combined group followed by artesunate monotherapy group. There was a significant increase in the apoptotic proteins P53 and slight increase in anti-apoptotic proteins Bcl-2 in the infected group compared to the control healthy group. A significant decrease and increase in P53 & Bcl-2 expressions respectively were observed in artesunate -praziquantel combined group compared to control infected group. Conclusion: artesunate-praziquantel combination is a potential upcoming chemotherapy for schistosomiasis mansoni. Both Bcl-2 and P53 are good markers assessing S. mansoni apoptosis, morbidity and chemotherapy efficacy.
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页码:193 / 203
页数:11
相关论文
共 37 条
[1]  
Abdel-Fattah Nashwa, 2011, Scientia Parasitologica, V12, P139
[2]   Artesunate Effect on Schistosome Thioredoxin Glutathione Reductase and Cytochrome c Peroxidase as New Molecular Targets in Schistosoma mansoni-infected Mice [J].
Abdin, Amany A. ;
Ashour, Dalia S. ;
Shoheib, Zeinab S. .
BIOMEDICAL AND ENVIRONMENTAL SCIENCES, 2013, 26 (12) :953-961
[3]  
[Anonymous], 2010, Schistosomiasis
[4]   Towards an understanding of the mechanism of action of praziquantel [J].
Aragon, Anthony D. ;
Imani, Reza A. ;
Blackburn, Vint R. ;
Cupit, Pauline M. ;
Melman, Sandra D. ;
Goronga, Tinopiwa ;
Webb, Thomas ;
Loker, Eric S. ;
Cunningham, Charles .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2009, 164 (01) :57-65
[5]  
Araujo N, 1999, Rev Soc Bras Med Trop, V32, P7
[6]   Apoptosis versus necrosis rate as a predictor in acute liver failure following acetaminophen intoxication compared with acute-on-chronic liver failure [J].
Bechmann, Lars P. ;
Marquitan, Guido ;
Jochum, Christoph ;
Saner, Fuat ;
Gerken, Guido ;
Canbay, Ali .
LIVER INTERNATIONAL, 2008, 28 (05) :713-716
[7]   Immunohistopathological and biochemical changes in Schistosoma mansoni-infected mice treated with artemether [J].
Botros, Sanaa S. ;
Mahmoud, Madiha R. ;
Moussa, Mona M. ;
Nosseir, Mona M. .
JOURNAL OF INFECTION, 2007, 55 (05) :470-477
[8]   Praziquantel efficacy in mice infected with PZQ non-susceptible S. mansoni isolate treated with artemether: parasitological, biochemical and immunohistochemical assessment [J].
Botros, Sanaa S. ;
Hammam, Olfat ;
Mahmoud, Madiha ;
Bergquist, Robert .
APMIS, 2010, 118 (09) :692-702
[10]   p53-family proteins and their regulators: hubs and spokes in tumor suppression [J].
Collavin, L. ;
Lunardi, A. ;
Del Sal, G. .
CELL DEATH AND DIFFERENTIATION, 2010, 17 (06) :901-911